| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308919 |
| Start |
987158:987158(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.871C>A |
| AA Mutation |
p.Leu291Met(p.L291M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308919 |
| Start |
985012:985012(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.400C>T |
| AA Mutation |
p.His134Tyr(p.H134Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308919 |
| Start |
987196:987196(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.909C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |